Regulatory Affairs and Patient Safety

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Regulatory Affairs and Patient Safety professional based in Brazil.

This role sits within a global clinical development environment focused on ensuring that life-changing therapies are developed, approved, and monitored with the highest standards of safety and regulatory compliance. You will contribute directly to improving patient outcomes by supporting regulatory submissions, product compliance activities, and pharmacovigilance processes across multiple therapeutic areas. The position offers exposure to both regulatory affairs and patient safety functions, allowing you to work across labeling, submissions, health authority interactions, and safety monitoring activities. You will collaborate with cross-functional teams in a highly regulated, mission-driven environment where accuracy, scientific rigor, and patient impact are central. The role also provides flexibility through remote work, enabling you to contribute to global healthcare innovation while maintaining work-life balance. This is an opportunity to play a meaningful part in advancing clinical research and ensuring therapies reach patients safely and efficiently.